Technical Service Manual
177 Pages
Preview
Page 1
TM
For use with List Numbers 12348-04 and 12618-04
Technical Service Manual
Hospira, Inc. 275 North Field Drive Lake Forest, IL 60045 USA
430-95424-006 (B, 2013-05)
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Plum A+3 Infusion System
Technical Service Manual
Change History Part Number
Description of Change
430-95424-005 (Rev. 09/10)
Fifth Issue
430-95424-006 (B, 2013-05)
Sixth Issue Update graphics to: - Remove Hospira copyright from Display and Keypad figures) (Sections 1 and 5).
Update Distal Air-in-Line test in the PVT
- Update Alarms Log and Setting the Time and Date figures with more current year (2011) (Section 1 only). Section 5, Distal Air-in-Line Test section: - Change DISTAL AIR A. BACKPRIME to N234 DISTAL AIR. -
Add Note about older versions.
Section 6, Troubleshooting: - Delete Morgan Hill return address information. Section 6, Error Codes Requiring Technical Service table, entries E378 and E379: - Add replace CPU PWA corrective actions. Section 6, Troubleshooting Procedures section: - Add Notes regarding operational alarm messages and unrestricted flow. - Add new section Unrestricted Flow to add unrestricted flow procedure with unrestricted flow warning and regulator closer caution (Unrestricted Flow section). Section 7, update procedure as follows: - Update Section 7, Cassette Door and Fluid Shield Replacement section: - Extensive revision to add steps, figures, cautions regarding unrestricted flow and the regulator closer. Section 8, Specifications: - Update air-in-line Air in Line Alarm (Air in Line Alarm for single air bolus to be 0.1 ml or larger) for single air bolus and cumulative air bolus (0.25 ml out of 4.9 ml). Back Page: - Delete Morgan Hill return address information.
Technical Service Manual
-
Update IEC symbols/descriptions.
-
Add “All Rights Reserved”.
Plum A+3 Infusion System
CHANGE HISTORY
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Plum A+3 Infusion System
Technical Service Manual
Contents Section 1 INTRODUCTION... 1.1 SCOPE... 1.2 CONVENTIONS... 1.3 COMPONENT DESIGNATORS... 1.4 ACRONYMS AND ABBREVIATIONS . . 1.5 USER QUALIFICATION... 1.6 ARTIFACTS... 1.7 INFUSION SYSTEM INSTALLATION . . 1.7.1 UNPACKING... 1.7.2 INSPECTION... 1.7.3 SELF TEST... 1.8 BIOMED SETTINGS... 1.8.1 IV PARAMETERS... 1.8.2 ALARMS LOG... 1.8.3 SETTING THE TIME AND DATE.
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. 1-1 . 1-1 . 1-2 . 1-2 . 1-3 . 1-5 . 1-5 . 1-5 . 1-6 . 1-6 . 1-6 . 1-8 . 1-10 . 1-12 . 1-13
Section 2 WARRANTY .
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2-1
SYSTEM OPERATING MANUAL
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3-1
THEORY OF OPERATION... 4.1 GENERAL DESCRIPTION... 4.2 ELECTRONIC SUBSYSTEM OVERVIEW... 4.2.1 CPU SUBSYSTEM... 4.2.1.1 CPU... 4.2.1.2 SYSTEM MEMORY ADDRESS MAP... 4.2.1.3 PROGRAMMABLE READ-ONLY MEMORY . 4.2.1.4 STATIC RANDOM ACCESS MEMORY . . . 4.2.1.5 CONTROL LOGIC... 4.2.1.6 LCD CONTROLLER... 4.2.1.7 LCD BACKLIGHT CONTROL... 4.2.1.8 LCD CONTRAST CONTROL... 4.2.1.9 REAL-TIME CLOCK... 4.2.1.10 VOLTAGE MONITOR WATCHDOG TIMER . 4.2.1.11 ANALOG-TO-DIGITAL CONVERTER . . . 4.2.1.12 DIGITAL-TO-ANALOG CONVERTER . . . 4.2.1.13 FRONT PANEL KEYPAD MATRIX... 4.2.1.14 FRONT PANEL [ON/OFF] KEY... 4.2.1.15 FRONT PANEL LED INDICATORS... 4.2.1.16 KEYPAD LOCKOUT INTERFACE... 4.2.1.17 NURSE CALL INTERFACE... 4.2.1.18 AUDIBLE INDICATORS... 4.2.1.19 BARCODE READER INTERFACE... 4.2.1.20 DATAPORT INTERFACE... 4.2.1.21 POWER SUPPLY INTERFACE... 4.2.1.22 MECHANISM INTERFACE...
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. 4-1 . 4-1 . 4-2 . 4-3 . 4-3 . 4-3 . 4-4 . 4-4 . 4-4 . 4-4 . 4-5 . 4-5 . 4-5 . 4-6 . 4-6 . 4-8 . 4-8 . 4-8 . 4-8 . 4-9 . 4-9 . 4-9 . 4-9 . 4-10 . 4-10 . 4-11
Technical Service Manual
Plum A+3 Infusion System
Section 3 Section 4
iii
CONTENTS
4.2.2
POWER SUPPLY SUBSYSTEM... 4.2.2.1 MAIN SWITCHING REGULATOR... 4.2.2.2 MAIN REGULATOR FAULT DETECTION. . 4.2.2.3 SYSTEM POWER... 4.2.2.4 AUXILIARY SUPPLIES... 4.2.2.5 POWER CONTROL... 4.2.2.6 BATTERY VOLTAGE MEASUREMENT. . . 4.2.2.7 BATTERY CHARGE/DISCHARGE CURRENT MEASUREMENT... 4.2.2.8 BATTERY CHARGER... 4.2.3 MECHANISM SUBSYSTEM... 4.2.3.1 MOTORS/MOTOR DRIVE... 4.2.3.2 MOTOR POSITION SENSORS... 4.2.3.3 V2_5 REFERENCE VOLTAGE... 4.2.3.4 AIR SENSORS... 4.2.3.5 PRESSURE SENSORS... 4.2.3.6 PRESSURE SENSOR CALIBRATION... 4.2.3.7 CASSETTE TYPE/PRESENCE SELECTION. . 4.2.3.8 SERIAL EEPROM... 4.3 PRINTED WIRING ASSEMBLIES... 4.3.1 POWER SUPPLY PWA... PERIPHERAL PWA... 4.3.2 4.3.3 PERIPHERAL INTERFACE PWA... 4.3.4 CPU PWA... 4.3.5 DRIVER PWA... 4.3.6 SWITCH PWA... 4.3.7 APP PWA... 4.4 REMOTE MOUNTED PERIPHERALS... 4.4.1 LCD... 4.4.2 SEALED LEAD ACID BATTERY... 4.4.3 BARCODE READER WAND... 4.5 MECHANICAL OVERVIEW... 4.5.1 CASSETTE... 4.5.2 MECHANISM ASSEMBLY... 4.5.2.1 MOTOR AND VALVE ASSEMBLIES... 4.5.2.2 A/B VALVE SUBSYSTEM... 4.5.2.3 INLET/OUTLET VALVE SUBSYSTEM . . . 4.5.2.4 PLUNGER DRIVE SUBSYSTEM...
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4-13 4-13 4-14 4-14 4-14 4-14 4-15
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4-15 4-16 4-16 4-16 4-18 4-18 4-19 4-20 4-22 4-22 4-22 4-23 4-23 4-24 4-24 4-25 4-25 4-26 4-26 4-27 4-27 4-27 4-27 4-27 4-28 4-30 4-30 4-30 4-31 4-31
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5-1 5-1 5-1 5-2 5-3 5-3 5-4 5-4 5-6 5-6 5-6 5-7 5-8 5-9
Section 5 MAINTENANCE AND SERVICE TESTS... 5.1 ROUTINE MAINTENANCE... 5.1.1 CLEANING AND SANITIZING... 5.2 PERFORMANCE VERIFICATION TEST... 5.2.1 EQUIPMENT REQUIRED... 5.2.2 INSPECTION... 5.2.3 TEST SETUP... SELF TEST... 5.2.4 5.2.5 CASSETTE ALARM TEST... 5.2.6 FREE FLOW TEST... 5.2.7 DISPLAY TEST... 5.2.8 KEYPAD VERIFICATION/FUNCTIONAL TEST 5.2.9 ALARM LOUDNESS TEST... 5.2.10 LOCKOUT SWITCH TEST...
Plum A+3 Infusion System
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CONTENTS
5.2.11 PROXIMAL OCCLUSION TEST . . 5.2.12 PROXIMAL AIR-IN-LINE TEST . . 5.2.13 DISTAL AIR-IN-LINE TEST... 5.2.14 DISTAL OCCLUSION TEST . . . 5.2.15 DELIVERY ACCURACY TEST . . . 5.2.16 NURSE CALL TEST... 5.2.17 ELECTRICAL SAFETY TEST . . . 5.2.18 END OF THE PVT... 5.3 PERIODIC MAINTENANCE INSPECTION . 5.4 BATTERY OPERATION OVERVIEW . . .
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. 5-9 . 5-10 . 5-11 . 5-11 . 5-13 . 5-13 . 5-14 . 5-15 . 5-15 . 5-16
TROUBLESHOOTING... 6.1 TECHNICAL ASSISTANCE... 6.2 WARNING MESSAGES... 6.3 ALARM MESSAGES AND ERROR CODES... 6.3.1 OPERATIONAL ALARM MESSAGES... 6.3.2 ERROR CODES REQUIRING TECHNICAL SERVICE 6.4 TROUBLESHOOTING PROCEDURES... 6.4.1 UNRESTRICTED FLOW...
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. 6-1 . 6-1 . 6-1 . 6-2 . 6-2 . 6-7 . 6-12 . 6-14
REPLACEABLE PARTS AND REPAIRS... 7.1 REPLACEABLE PARTS... 7.2 REPLACEMENT PROCEDURES... 7.2.1 SAFETY AND EQUIPMENT PRECAUTIONS... 7.2.2 REQUIRED TOOLS AND MATERIALS... 7.2.3 RUBBER FOOT PAD REPLACEMENT... 7.2.4 BATTERY, WIRE HARNESS, DOOR, AND DOOR PAD REPLACEMENT... 7.2.5 AC POWER CORD, RETAINER, AND VELCRO STRAP REPLACEMENT... 7.2.6 SEPARATING THE FRONT ENCLOSURE, REAR ENCLOSURE, AND MAIN CHASSIS ASSEMBLY... PERIPHERAL INTERFACE ASSEMBLY REPLACEMENT... 7.2.7 7.2.8 PERIPHERAL PWA REPLACEMENT... 7.2.9 PERIPHERAL COMPONENT REPLACEMENT... 7.2.9.1 VOLUME CONTROL KNOB REPLACEMENT... 7.2.9.2 PERIPHERAL COVER REPLACEMENT... 7.2.10 FRONT/REAR ENCLOSURE GASKET REPLACEMENT... 7.2.11 LOWER FRONT ENCLOSURE GASKET REPLACEMENT... 7.2.11.1 EMI GASKET REPLACEMENT... 7.2.11.2 KEYPAD GASKET REPLACEMENT... 7.2.11.3 TOP SEAL GASKET REPLACEMENT... 7.2.12 REAR ENCLOSURE ASSEMBLY COMPONENT REPLACEMENT . 7.2.12.1 POLE CLAMP ASSEMBLY AND BACKING PLATE REPLACEMENT... 7.2.12.2 INTERNAL AC POWER CORD REPLACEMENT . . . 7.2.12.3 AC CONNECTOR REPLACEMENT... 7.2.12.4 FUSE REPLACEMENT... 7.2.12.5 REAR ENCLOSURE GASKET REPLACEMENT... 7.2.13 MINIPOLE ASSEMBLY REPLACEMENT...
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7-1 7-1 7-1 7-1 7-2 7-2
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. 7-19 . 7-20 . 7-20 . 7-21 . 7-22 . 7-22
Section 6
Section 7
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Plum A+3 Infusion System
CONTENTS
7.2.14
MAIN CHASSIS ASSEMBLY COMPONENT REPLACEMENT . . . 7.2.14.1 POWER SUPPLY PWA REPLACEMENT... 7.2.14.2 KEYPAD REPLACEMENT... 7.2.14.3 DISPLAY ASSEMBLY REPLACEMENT... 7.2.14.4 CPU/DRIVER CABLE REPLACEMENT... 7.2.14.5 MOTOR POWER CABLE REPLACEMENT... 7.2.14.6 CPU PWA REPLACEMENT... 7.2.14.7 PIEZO ALARM ASSEMBLY REPLACEMENT... 7.2.14.8 MECHANISM ASSEMBLY REPLACEMENT... 7.2.14.9 CASSETTE DOOR AND FLUID SHIELD REPLACEMENT . 7.2.14.10 OPENER HANDLE ASSEMBLY REPLACEMENT...
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7-23 7-26 7-26 7-27 7-28 7-31 7-31 7-32 7-33 7-34 7-39
Section 8 SPECIFICATIONS .
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8-1
Section 9 DRAWINGS .
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9-1
Appendix .
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A-1
Index .
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I-1
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Figures Figure 1-1. Figure 1-2. Figure 1-3. Figure 1-4. Figure 1-5. Figure 1-6. Figure 1-7. Figure 4-1. Figure 4-2. Figure 4-3. Figure 4-4. Figure 4-5. Figure 4-6. Figure 4-7. Figure 4-8. Figure 4-9. Figure 5-1. Figure 5-2. Figure 5-3. Figure 5-4. Figure 5-5. Figure 6-1. Figure 7-1. Figure 7-2. Figure 7-3. Figure 7-4. Figure 7-5. Figure 7-6. Figure 7-7. Figure 7-8.
Display and Keypad... Biomed Settings... IV Parameters... Common IV Parameters... Macro IV Parameters... Alarms Log... Setting the Time and Date... Electronic Functional Diagram... Serial Interface to ADC... System Startup and Shutdown Timing, Battery Powered . . . Stepper Motor Coils... Air Sensor Block Diagram... Pressure Sensor Excitation and Amplifier Block Diagram . . . Major Elements of the Dual-Channel Cassette... Fluid Path in the Cassette... Mechanism Valve Pins and Sensor Locations... Display and Keypad... Primary Screen... Rear View... Special Cassettes with Bubble Sensor Tips Removed... Distal Occlusion Test Setup... Regulator Closer... Bottom View... AC Power Cord Assembly and Battery Assembly... Rear Enclosure, Main Chassis, and Front Enclosure... Screw Placement Sequence... Peripheral Interface Assembly and Peripheral PWAs... Peripheral Interface Assembly Components... Lower Front Enclosure Gaskets... External Rear Enclosure Assembly Components...
Plum A+3 Infusion System
vi
... 1-7 ... 1-9 ... 1-10 ... 1-11 ... 1-11 ... 1-12 ... 1-13 ... 4-2 ... 4-7 ... 4-15 ... 4-17 ... 4-19 ... 4-21 ... 4-29 ... 4-29 ... 4-31 ... 5-5 ... 5-7 ... 5-8 ... 5-11 ... 5-12 ... 6-14 ... 7-3 ... 7-5 ... 7-8 ... 7-9 ... 7-11 ... 7-13 ... 7-15 ... 7-17
Technical Service Manual
CONTENTS
Figure 7-9. Figure 7-10. Figure 7-11. Figure 7-11. Figure 7-12. Figure 7-13. Figure 7-13. Figure 7-14. Figure 7-15. Figure 7-16. Figure 7-17. Figure 7-18. Figure 9-1. Figure 9-1. Figure 9-2. Figure 9-3. Figure 9-4. Figure 9-4. Figure 9-5. Figure 9-6. Figure 9-6. Figure 9-7. Figure 9-8. Figure 9-9. Figure 9-10.
Internal Rear Enclosure Assembly Components... Minipole Assembly... Main Chassis Components (1 of 2)... Main Chassis Components (2 of 2)... CPU/Driver Cable Routing... Ferrite Tape Positioning (1 of 2)... Ferrite Tape Positioning (2 of 2)... Fluid Shield Tab... Normal Fluid Shield Tab Before and After Assembly is Seated . Close-up Views of Normal (left) and Bent (right) Fluid Shield . Fluid Shield Replacement... Cassette Door and Opener Handle Assembly Replacement . . Illustrated Parts Breakdown (1 of 2)... Illustrated Parts Breakdown (2 of 2)... Front Enclosures, Rear Enclosure, and Main Chassis Assembly . Front Enclosure Assemblies... Rear Enclosure Assembly (1 of 2)... Rear Enclosure Assembly (2 of 2)... Peripheral Interface Assembly... Main Chassis Assembly (1 of 2)... Main Chassis Assembly (2 of 2)... CPU PWA, Display, and Keypad... CPU PWA and Main Chassis... AC Power Cord, Retainer, Batteries, and Minipole... Mechanism Assembly...
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. 7-18 . 7-23 . 7-24 . 7-25 . 7-29 . 7-30 . 7-30 . 7-35 . 7-36 . 7-36 . 7-37 . 7-38 . 9-5 . 9-7 . 9-9 . 9-11 . 9-13 . 9-15 . 9-17 . 9-19 . 9-21 . 9-23 . 9-25 . 9-27 . 9-29
Tables Table 1-1. Table 1-2. Table 4-1. Table 4-2. Table 4-3. Table 4-4. Table 4-5. Table 4-6. Table 4-7. Table 4-8. Table 4-9. Table 4-10. Table 5-1. Table 5-2. Table 6-1. Table 6-2. Table 6-3. Table 6-4. Table 9-1. Table 9-2. Table A-1. Table A-2. Table A-3. Table A-4.
Conventions... 1-2 System Configuration Data... 1-9 Analog Inputs... 4-7 Keypad Map... 4-8 CPU-Power Supply Interface... 4-10 CPU-Mechanism Interface Signals... 4-11 Power Supply PWA Interface Connections... 4-23 Peripheral PWA Interface Connections... 4-24 Peripheral Interface PWA Interface Connections... 4-24 CPU PWA Interface Connections... 4-25 Driver PWA Interface Connections... 4-25 APP PWA Interface Connections... 4-26 Cleaning Solutions... 5-2 Electrical Safety Measurements... 5-14 Warning Messages... 6-2 Operational Alarm Messages and Corrective Actions... 6-3 Error Codes Requiring Technical Service... 6-7 Troubleshooting with the PVT... 6-12 Drawings... 9-1 IPB for the Infuser... 9-1 Guidance and Manufacturer’s Declaration - Electromagnetic Emissions... A-1 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity ... A-2 Guidance and Manufacturer’s Declaration Electromagnetic Immunity for Life-Supporting Equipment and Systems ... A-3 Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the Infusion System... A-5
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Technical Service Manual
Section 1
INTRODUCTION The Plum A+™ 3 infusion system is designed to meet the growing demand for hospital wide device standardization, and serves a wide range of general floor and critical care needs. The infusion system consists of three component infusers, designated line 1, line 2, and line 3. By incorporating three lines into one unit, the Plum A+3 provides three primary lines, three secondary lines, and piggyback fluid delivery capabilities. Compatibility with the LifeCare™ 5000 PlumSet™ administration sets and accessories makes the Plum A+3 a convenient and cost-effective infusion system.
1.1
SCOPE This manual is organized into the following sections:
Section 1 Introduction
Section 2 Warranty
Section 3 System Operating Manual
Section 4 Theory of Operation
Section 5 Maintenance and Service Tests
Section 6 Troubleshooting
Section 7 Replaceable Parts and Repairs
Section 8 Specifications
Section 9 Drawings
Appendix
Index
Technical Service Bulletins
If a problem in device operation cannot be resolved using the information in this manual, contact Hospira (see Section 6.1). Specific instructions for operating the device are contained in its respective System Operating Manual. The terms “infusion system”, “infuser”, and “device” are used interchangeably throughout the manual. Figures are rendered as graphic representations to approximate actual product. Therefore, figures may not exactly reflect the product. Screen representations are examples only, and do not necessarily reflect the most current software version.
Plum A+3 Infusion System
1-1
Technical Service Manual
SECTION 1 INTRODUCTION
1.2
CONVENTIONS The conventions listed in Table 1-1 are used throughout this manual. Table 1-1. Convention
Conventions
Application
Example
Blue italic
Reference to a section, figure, table, or website
(see Section 6.1)
[ALL CAPS] in brackets
Touchswitches, keys, buttons
[START]
ALL CAPS Bold
Screens and displayed messages
CASSETTE TEST IN PROGRESS
Red Bold
Warnings and Cautions
CAUTION: Use proper ESD grounding techniques when handling components.
Throughout this manual, warnings, cautions, and notes are used to emphasize important information as follows: WARNING: A WARNING CONTAINS SPECIAL SAFETY EMPHASIS AND MUST BE OBSERVED AT ALL TIMES. FAILURE TO OBSERVE A WARNING MAY RESULT IN PATIENT INJURY AND BE LIFE-THREATENING. CAUTION: A CAUTION usually appears in front of a procedure or statement. It contains information that could prevent hardware failure, irreversible damage to equipment, or loss of data.
d Note: A note highlights information that helps explain a concept or procedure. 1.3
COMPONENT DESIGNATORS Components are indicated by alpha-numeric designators, as follows: Battery
BT
Diode
D
Resistor
R
Capacitor
C
Fuse
F
Switch
SW
Crystal
Y
Integrated Circuit
U
Transistor
Q
The number following the letter is a unique value for each type of component (e.g., R1, R2).
d Note: Alpha-numeric designators may be followed with a dash (-) number that indicates a pin number for that component. For example, U15-13 is pin 13 of the encoder chip [U15] on the interface PWA.
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1-2
Plum A+3 Infusion System
1.4
ACRONYMS AND ABBREVIATIONS
1.4
ACRONYMS AND ABBREVIATIONS Acronyms and abbreviations used in this manual are as follows: A Ampere AC Alternating current A/D Analog-to-digital ADC Analog-to-digital converter APP Air, pressure, and pin BCR Barcode reader CCA Clinical care area CCFT Cold cathode fluorescent tube CMOS Complementary metal-oxide semiconductor CPU Central processing unit DAC Digital-to-analog converter DC Direct current DIP Dual in-line package DMA Direct memory access DMM Digital multimeter DPM Digital pressure meter ECG Electrocardiograph EEG Electroencephalogram EEPROM Electrically erasable/programmable read-only memory EMG Electromyogram EMI Electromagnetic interference ESD Electrostatic discharge ETO Ethylene oxide FPGA Field programmable gate array FSR Force sensing resistor hr Hour Hz Hertz ID Identification I/O Input/output IPB Illustrated parts breakdown IV Intravenous KB Kilobyte kHz Kilohertz KVO Keep vein open lbs Pounds LCD Liquid crystal display
Plum A+3 Infusion System
1-3
Technical Service Manual
SECTION 1 INTRODUCTION
LED Light emitting diode L/S Line select MB Megabyte MHz Megahertz min Minute mL Milliliter mL/hr Milliliter per hour MMIO Memory-mapped input/output MOSFET Metal-oxide semiconductor field-effect transistor ms Millisecond nF nanofarad Op-amp Operational amplifier pF picofarad PROM Programmable read-only memory PVT Performance verification test PWA Printed wiring assembly PWM Pulse width modulator RAM Random-access memory rms Root-mean-square RTC Real-time clock SCC Serial communication controller SCP Serial communication port SMT Surface mount technology SPI Serial peripheral interface SRAM Static random access memory TQFP Thin quad flat pack V Volt VAC Volts AC VCC Collector supply voltage VCO Voltage-controlled oscillator VDC Volts DC VSC 5 VDC supply circuitry VSO Voltage sweep oscillator VTBI Volume to be infused WDI Watchdog input
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Plum A+3 Infusion System
1.5 USER QUALIFICATION
1.5
USER QUALIFICATION The Plum A+3 must be used at the direction of or under the supervision of licensed physicians or certified healthcare professionals who are trained in the use of the infusion system and the administration of parenteral and enteral fluids and drugs, and whole blood or red blood cell components. Training should emphasize preventing related IV complications, including appropriate precautions to prevent accidental infusion of air. The epidural route can be used to provide anesthesia or analgesia.
1.6
ARTIFACTS Nonhazardous, low-level electrical potentials are commonly observed when fluids are administered using infusion devices. These potentials are well within accepted safety standards, but may create artifacts on voltage-sensing equipment such as ECG, EMG, and EEG machines. These artifacts vary at a rate that is associated with the infusion rate. If the monitoring machine is not operating correctly or has loose or defective connections to its sensing electrodes, these artifacts may be accentuated so as to simulate actual physiological signals. To determine if the abnormality in the monitoring equipment is caused by the infuser instead of some other source in the environment, set the device so that it is temporarily not delivering fluid. Disappearance of the abnormality indicates that it was probably caused by electronic noise generated by the infuser. Proper setup and maintenance of the monitoring equipment should eliminate the artifact. Refer to the appropriate monitoring system documentation for setup and maintenance instructions.
1.7
INFUSION SYSTEM INSTALLATION CAUTION: Infusion system damage may occur unless proper care is exercised during product unpacking and installation. CAUTION: Infusion system performance may be degraded by electromagnetic interference (EMI) from devices such as electrosurgical units, cellular phones, and two-way radios. Operation of the infusion system under such conditions should be avoided.
Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC standards (e.g., IEC 60601-1 for medical equipment). Furthermore, all configurations shall comply with the system standard IEC 60601-1-1. Any person who connects additional equipment to the signal input or output part is configuring a medical system, and is therefore responsible for ensuring that the system complies with the requirements of IEC 60601-1-1. If in doubt, contact Hospira. Infusion system installation consists of unpacking, inspection, and self test.
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SECTION 1 INTRODUCTION
1.7.1
UNPACKING Inspect the shipping container as detailed in Section 1.7.2. Use care when unpacking the infusion system. Retain the packing slip and save all packing materials in the event it is necessary to return the infusion system to the factory. Verify the shipping container contains a copy of the System Operating Manual.
1.7.2
INSPECTION Inspect the shipping container for damage. Should any damage be found, contact the delivering carrier immediately. CAUTION: Do not use the infusion system if it appears to be damaged. Should damage be found, contact Hospira. Inspect the infusion system periodically for signs of defects such as worn accessories, broken connections, or damaged cable assemblies. Also inspect the infuser after repair or during cleaning. Replace any damaged or defective external parts.
1.7.3
SELF TEST When performing the self test, line 1, line 2, and line 3 must be tested. However, if appropriate, the test may be performed on all lines concurrently. CAUTION:
Do not place the infuser in service if the self test fails.
If an alarm condition occurs during the self test, cycle the power and repeat the self test. If the alarm condition recurs, note the message and take corrective action (see Section 6), then repeat the self test. If the alarm condition continues to recur, remove the infuser from service and contact Hospira.
d Note: Do not place the infuser in service if the battery is not fully charged. To make certain the battery is fully charged, connect the infuser to AC power for six hours.
d Note: When plugging the device into an AC power outlet, grasp the AC power
cord plug and use a forward motion into the socket. Do not use a sideways motion. When unplugging the device, grasp the AC power cord plug and pull straight out. Do not pull out using the power cord cable and do not pull out at an angle.
d Note: Records prior to the date the infuser is received may be from
the manufacturing process. Disregard any events from dates prior to receipt of the infuser.
To perform the self test, see Figure 1-1, and proceed as follows: 1. Connect the AC power cord to a grounded AC outlet. Verify the Charge/Line indicator CHARGE illuminates and an alarm tone sounds. 2. Without a cassette installed, press [ON/OFF] to turn on the infuser.
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Plum A+3 Infusion System
1.7
INFUSION SYSTEM INSTALLATION
3. The LCD screen briefly displays the SELF TEST screen (see Figure 1-1). If the SELF TEST screen does not appear, contact Hospira. 4. After the self test is complete, the message INSERT PLUM SET CLOSE LEVER appears. 5. Verify the time and date. To set the time and date, see Section 1.8.3. Open the cassette door and insert a primed cassette. Close the cassette door. The cassette test is complete when the CASSETTE TEST IN PROGRESS message disappears.
d Note: The message
MECHANISM INITIALIZATION IN PROGRESS may briefly
appear prior to the CASSETTE TEST IN PROGRESS message.
6. The CLEAR SETTINGS? message may appear. Press the [YES] softkey. 7. Press [ON/OFF] to turn off the infuser.
LINE FLOW INDICATORS A B
HOSPIRA Plum A+ Version X.XX - MM/DD/YY
STATUS REGION
2009 System Self Test In Progress
WORKING REGION
MESSAGE REGION SOFTKEY LABEL REGION
START STOP CHARGE
LINE INDICATOR
ON / OFF
1 4 7 CLEAR
Figure 1-1.
Plum A+3 Infusion System
2 5 8 0
3 6 9 .
SOFT KEYS
SELECT KEYPAD
SILENCE
Display and Keypad
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Technical Service Manual
SECTION 1 INTRODUCTION
1.8
BIOMED SETTINGS The BIOMED SETTINGS screens contain the following options that can be changed or reviewed by qualified personnel: - IV screen parameters - Alarms log - Set time and date All infusers (new or refurbished) are shipped with factory settings (see Table 1-2).
d Note: Biomed screens do not time out for the alarm or alarm. d Note: The battery will not be detected in the Biomed service mode. Infuser Idle
No Action
To access the Biomed settings, proceed as follows: 1. Open the door and turn on the device. The infusion system will perform a self test. 2. After the self test is complete, the message INSERT PLUM SET CLOSE LEVER appears. 3. Press the decimal [.] key, then [START], and verify the BIOMED SETTINGS screen is displayed (see Figure 1-2).
d Note: The
BIOMED SETTINGS screen may display [CHANGE BATTERY]. The [CHANGE BATTERY] softkey does not appear on earlier versions of the Plum A+3.
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Plum A+3 Infusion System
1.8
Table 1-2.
BIOMED SETTINGS
System Configuration Data
Data
Options Range
Factory Setting
Maximum macro IV mode delivery rate
0.1 - 99.9 mL/hr and 100 - 999 mL/hr
999 mL/hr
Macro distal occlusion alarm (pressure level)
1 to 15 psi
6 psi
Deliver together enable
Concurrent or Piggyback
Piggyback
Delayed start/standby enable
Yes or No
Yes
Continue rate
Rate or KVO
KVO
Nurse callback default
Yes or No
No
Time
(24 hr) 00:00 - 23:59 in one minute increments
Factory time
Date
1/1/2002 - 12/31/2098
Factory date
BIOMED SETTINGS IV Screen Parameters Alarm Log Set Time and Date
Select, then Choose Change Battery Figure 1-2.
Plum A+3 Infusion System
Choose
Biomed Settings
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SECTION 1 INTRODUCTION
1.8.1
IV PARAMETERS The IV Parameters screen contains Common IV Parameters and Macro IV Parameters (see Figure 1-3). To change the IV parameters see Figure 1-4 and Figure 1-5, then proceed as follows: 1. Access the BIOMED SETTINGS screen as described in Section 1.8. 2. Select IV Screen Parameters, and press [CHOOSE]. 3. Select the parameters to be changed, and press [CHOOSE]. 4. Using the [CHANGE VALUE] softkey, select the desired value, and press [ENTER]. 5. Repeat step 3 and step 4 for each parameter to be changed. 6. If there are no other changes, turn off the infuser.
BIOMED SETTINGS IV Parameters Common IV Parameters Macro IV Parameters
Select, then Choose Choose Figure 1-3.
Technical Service Manual
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IV Parameters
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Plum A+3 Infusion System